Canonical Allele Identifier: CA2636444094

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18159179-ACCCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159182_18159185del , CM000679.2:g.18159182_18159185del	GRCh38
NC_000017.10:g.18062496_18062499del , CM000679.1:g.18062496_18062499del	GRCh37
NC_000017.9:g.18003221_18003224del	NCBI36
NG_011634.1:g.55477_55480del
NG_011634.2:g.55477_55480del

Transcript Alleles

HGVS	Amino-acid change
ENST00000642418.1:n.1495-93_1495-90del
ENST00000643693.1:n.959-93_959-90del
ENST00000644795.1:c.949-93_949-90del	ENSP00000495720.1:n.949-93_949-90del
ENST00000646782.1:n.1891-93_1891-90del
ENST00000647165.2:c.9157-93_9157-90del MANE Select	ENSP00000495481.1:n.9157-93_9157-90del
ENST00000651214.1:n.1662-93_1662-90del
ENST00000205890.9:c.9157-93_9157-90del	ENSP00000205890.5:n.9157-93_9157-90del
ENST00000418233.7:c.949-93_949-90del	ENSP00000408800.3:n.949-93_949-90del
ENST00000433411.7:n.94-93_94-90del
ENST00000445289.6:n.316+1282_316+1285del
ENST00000556535.5:c.19-93_19-90del	ENSP00000451782.1:n.19-93_19-90del
ENST00000557190.5:n.59-93_59-90del
ENST00000557655.5:c.19-93_19-90del	ENSP00000451925.1:n.19-93_19-90del
ENST00000578472.5:c.19-93_19-90del	ENSP00000467989.1:n.19-93_19-90del
ENST00000615845.4:c.9157-93_9157-90del	ENSP00000481642.1:n.9157-93_9157-90del
NM_016239.3:c.9157-93_9157-90del	NP_057323.3:n.9157-93_9157-90del
XM_011523921.1:c.9151-93_9151-90del	XP_011522223.1:n.9151-93_9151-90del
XM_017024714.2:c.9097-93_9097-90del	XP_016880203.1:n.9097-93_9097-90del
XM_017024715.2:c.9160-93_9160-90del	XP_016880204.1:n.9160-93_9160-90del
NM_016239.4:c.9157-93_9157-90del MANE Select	NP_057323.3:n.9157-93_9157-90del